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81.
Serra Mariangela Cuccu Roberta Ghiani Cristina A. Pisu M. Giuseppina Murgia Antonella Biggio Giovanni 《Neurochemical research》1997,22(6):693-697
The transfer of tolerance between drugs may indicate a common mode of action. The development of cross-tolerance to the anticonvulsant effect of felbamate after long-term treatment of mice with diazepam, a positive modulator of -aminobutyric acid (GABA)-mediated transmission, was therefore studied in order to clarify the mechanism of this action of felbamate. A challenge injection of felbamate, administered 36 h after the last dose of chronic diazepam treatment, antagonized convulsions elicited by administration of isoniazid. In contrast, felbamate had no effect on the isoniazid-induced increase in t-[35S]butylbicyclophosphorothionate binding to cerebral cortical membranes of diazepam-tolerant mice. These results suggest that the action of felbamate on GA-BAergic transmission is not required for the anticonvulsant effect of this drug. This conclusion is consistent with studies that have indicated that the antiepileptic activity of felbamate depends on its modulatory activity at excitatory amino acid receptors. 相似文献
82.
Tumour‐associated macrophages correlate with microvascular bed extension in colorectal cancer patients 下载免费PDF全文
Ilaria Marech Michele Ammendola Rosario Sacco Giuseppe Sammarco Valeria Zuccalà Nicola Zizzo Christian Leporini Maria Luposella Rosa Patruno Gianfranco Filippelli Emilio Russo Mariangela Porcelli Cosmo Damiano Gadaleta Giovambattista De Sarro Girolamo Ranieri 《Journal of cellular and molecular medicine》2016,20(7):1373-1380
Tumour‐associated macrophages (TAMs) represent pivotal components of tumour microenvironment promoting angiogenesis, tumour progression and invasion. In colorectal cancer (CRC), there are no conclusive data about the role of TAMs in angiogenesis‐mediated tumour progression. In this study, we aimed to evaluate a correlation between TAMs, TAM immunostained area (TAMIA) microvascular density (MVD), endothelial area (EA) and cancer cells positive to VEGF‐A (CCP‐VEGF‐A) in primary tumour tissue of locally advanced CRC patients undergone to radical surgery. A series of 76 patients with CRC were selected and evaluated by immunohistochemistry and image analysis. An anti‐CD68 antibody was employed to assess TAMs and TAMIA expression, an anti‐CD34 antibody was utilized to detect MVD and EA expression, whereas an anti‐VEGF‐A antibody was used to detect CCP‐VEGF‐A; then, tumour sections were evaluated by image analysis methods. The mean ± S.D. of TAMs, MVD and CCP‐VEGF‐A was 65.58 ± 21.14, 28.53 ± 7.75 and 63% ± 37%, respectively; the mean ± S.D. of TAMIA and EA was 438.37 ± 124.14μ2 and 186.73 ± 67.22μ2, respectively. A significant correlation was found between TAMs, TAMIA, MVD and EA each other (r ranging from 0.69 to 0.84; P ranging from 0.000 to 0.004). The high level of expression of TAMs and TAMIA in tumour tissue and the significant correlation with both MVD and EA illustrate that TAMs could represent a marker that plays an important role in promoting angiogenesis‐mediated CRC. In this context, novel agents killing TAMs might be evaluated in clinical trials as a new anti‐angiogenic approach. 相似文献
83.
Emiliano Altamura Monica Borgatti Alessia Finotti Jessica Gasparello Roberto Gambari Mariangela Spinelli Rosa Castaldo Nicola Altamura 《PloS one》2016,11(4)
Nonsense mutations generate in-frame stop codons in mRNA leading to a premature arrest of translation. Functional consequences of premature termination codons (PTCs) include the synthesis of truncated proteins with loss of protein function causing severe inherited or acquired diseases. A therapeutic approach has been recently developed that is based on the use of chemical agents with the ability to suppress PTCs (read-through) restoring the synthesis of a functional full-length protein. Research interest for compounds able to induce read-through requires an efficient high throughput large scale screening system. We present a rapid, sensitive and quantitative method based on a dual-fluorescence reporter expressed in the yeast Saccharomyces cerevisiae to monitor and quantitate read-through at PTCs. We have shown that our novel system works equally well in detecting read-through at all three PTCs UGA, UAG and UAA. 相似文献
84.
Mariangela Serra Enrico Sanna Alessandra Concas Cristina Foddi Giovanni Biggio 《Neurochemical research》1991,16(1):17-22
We report earlier that isoniazid and foot-shock stress individually increase the maximal number of [35S]TBPS binding sites (Bmax) measured ex vivo in unwashed membranes from rat cerebral cortex and that the increase due to both treatments are prevented by pretreatment in vivo with diazepam which alone induced a significant decrease in the total number of [35S]TBPS binding sites. In the present paper, the effect of stress was studied on both the increase in [35S]TBPS binding and the convulsant activity induced by isoniazid in unstressed rats. Isoniazid induced a time dependent increase in [35S]TBPS binding. The isoniazid-induced increase in [35S]TBPS binding was markedly potentiated by foot-shock stress. Moreover, foot-shock stress markedly reduced the latency to the appearance of generalized seizures induced by isoniazid (300 mg/kg s.c.). The results provide evidence that the in vivo inhibition of GABAergic transmission elicited by isoniazid results in an increase of [35S]TBPS binding in the rats cerebral cortex. The finding that stress, like isoniazid, enhances [35S]TBPS binding suggests that this treatment also inhibits the function of GABAergic synapses. 相似文献
85.
Mariangela Hungria Richard J. Thomas 《World journal of microbiology & biotechnology》1987,3(4):411-419
Summary In an experiment performed under greenhouse conditions usingPhaseolus vulgaris cv. Carioca inoculated withRhizobium strain CO5, effects of cotyledons and mineral nitrogen on the initial process of nitrogen assimilation were evaluated. Plants were maintained intact or had either both or half of both cotyledons removed six days after planting. Levels of mineral nitrogen corresponded to the addition of 0 or 1.5 mg N/plant/day three days before each of the four harvests (8, 10, 12 and 14 days after planting). Cotyledon removal generally decreased nodule number and dry weight and total nitrogenase activity, although there was no effect on specific nodule efficiency, but the nitrate reductase activity was increased in both shoots and roots. Mineral nitrogen decreased nodulation and nitrogenase activity when applied 9 and 11 days after planting, but increased shoot and root nitrate reductase activity and total nitrogen incorporation, indicating that plants could be nitrogen limited during the initial period of growth.
Resumen En un experimento realizado en invernadero conPhaseolus vulgaris, cv. Carioca, inoculado conRhizobium (cepa CO5) fue evaluado los efectos de los cotiledones y del nitrógeno mineral en el proceso inicial de la assimilación de N. Las plantas fueron mantenidas intactas o con la mitad o todos los cotiledones retirados a los 6 dias despues de la siembra (DDS). El N mineral fue aplicado en la dosis de 0 ó 1.5 mg N/planta/dia, 3 dias antes de cada una de los 4 casechas realizadas (8, 10, 12 y 14 DDS). La retirada de los cotiledones generalmente disminuyó el número y el peso seco de los nódulos y la actividad de la nitrogenase, mas não hubo influencia en la eficiencia específica de los nódulos. La actividad de la nitrato reductasa aumentó tanto en la parte aérea como en las raíces. El nitrógeno mineral disminuyó la nodulación y la actividad de la nitrogenasa cuando la aplicación ocurrió a los 9 y 11 DDS, mas aumentó la actividad de la nitrato reductasa de las raíces y de la parte aérea, asi como el contenido de N en la planta, indicando que estas podrian estar limitadas por nitrógeno en la fase inicial de crescimento.
Résumé Dans une expérimentation réalisée dans les conditions de serre au moyen dePhaseolus vulgaris cv Carioca inoculée avec la souche CO5 deRhizobium, on a évalué les effets de cotylédons et de l'azote minéral sur le processus initial de l'assimilation azotée. Les plants ont été soit maintenus intacts soit amputés des deux ou de la moitié des deux cotylédons, 6 jours après la plantation. Les teneurs en azote minéral correspondaient à l'ajout de 0 ou 1.5 mg d'azote par plant et par jour, trois jours avant chacune des 4 récoltes (8, 10, 12 et 14 jours après la plantation). L'amputation de cotyledon diminue d'une manière générale le nombre de nodules, le poids sec et l'activité totale de nitrogénase, bien qu'il n'y ait aucun effet sur l'efficience spécifique de nodule mais l'activité de nitrate réductase était augmentée tant dans les pousses que dans les racines. L'azote minéral a déterminé la nodulation et l'activité de nitrogénase lorsque l'application avait lieu les 9ème et 11ème jours après la plantation, mais elle a augmenté l'activité de nitrate réductase chez les pousses et les racines ainsi que l'incorporation totale d'azote, indiquant par là que la plante pouvait être limitée en azote durant la période initiale de croissance.相似文献
86.
Daniela Rossi Mariangela Urbano Alice Pedrali Massimo Serra Daniele Zampieri Maria Grazia Mamolo Christian Laggner Caterina Zanette Chiara Florio Dirk Schepmann Bernard Wuensch Ornella Azzolina Simona Collina 《Bioorganic & medicinal chemistry》2010,18(3):1204-1212
In order to investigate the molecular features involved in sigma receptors (σ-Rs) binding, new compounds based on arylalkylaminoalcoholic, arylalkenyl- and arylalkylaminic scaffolds were synthesized and their affinity towards σ1- and σ2-Rs subtypes was evaluated. The most promising compounds were also screened for their affinity at μ-opioid, δ-opioid and κ-opioid receptors. Biological results are herein presented and discussed. 相似文献
87.
da Silva LM Galbiatti AL Ruiz MT Raposo LS Maniglia JV Pavarino EC Goloni-Bertollo EM 《Molecular biology reports》2012,39(2):887-893
Alterations in folate metabolism may contribute to the process of carcinogenesis by influencing DNA methylation and genomic
stability. Polymorphisms in genes encoding enzymes involved in this pathway may alter enzyme activity and consequently interfere
in concentrations of homocysteine and S-adenosylmethionine that are important for DNA synthesis and cellular methylation reactions.
The objectives were to investigate MTHFD1 G1958A, BHMT G742A, TC2 C776G and TC2 A67G polymorphisms involved in folate metabolism on head and neck cancer risk and the association between these polymorphisms
with risk factors. Polymorphisms were investigated in 762 individuals (272 patients and 490 controls) by polymerase chain
reaction–restriction fragment length polymorphism (PCR–RFLP) and Real Time-PCR. Chi-square and Multiple logistic regression
were used for the statistical analysis. Multiple logistic regression showed that tobacco and male gender were predictors for
the disease (P < 0.05). Hardy–Weinberg equilibrium showed that the genotypic distributions were in equilibrium for both groups in all polymorphisms
studied. The BHMT 742GA or AA genotypes associated with tobacco consumption (P = 0.016) increase the risk for head and neck squamous cell carcinoma (HNSCC). The present study suggests that BHMT 742GA polymorphism associated to tobacco modulate HNSCC risk. However, further investigation of gene–gene interactions in
folate metabolism and studies in different populations are needed to investigate polymorphisms and HNSCC risk. 相似文献
88.
Cláudio de Oliveira Cunha Luiz Fernando Goda Zuleta Luiz Gonzaga Paula de Almeida Luciane Prioli Ciapina Wardsson Lustrino Borges Rosa Maria Pitard José Ivo Baldani Rosangela Straliotto Sérgio Miana de Faria Mariangela Hungria Benildo Sousa Cavada Fábio Martins Mercante Ana Tereza Ribeiro de Vasconcelos 《Journal of bacteriology》2012,194(23):6675-6676
The genus Burkholderia represents a challenge to the fields of taxonomy and phylogeny and, especially, to the understanding of the contrasting roles as either opportunistic pathogens or bacteria with biotechnological potential. Few genomes of nonpathogenic strains, especially of diazotrophic symbiotic bacteria, have been sequenced to improve understanding of the genus. Here, we contribute with the complete genome sequence of Burkholderia phenoliruptrix strain BR3459a (CLA1), an effective diazotrophic symbiont of the leguminous tree Mimosa flocculosa Burkart, which is endemic to South America. 相似文献
89.
Mariangela Urbano Miguel Guerrero Jian Zhao Subash Velaparthi S. Adrian Saldanha Peter Chase Zhiwei Wang Olivier Civelli Peter Hodder Marie-Therese Schaeffer Steven Brown Hugh Rosen Edward Roberts 《Bioorganic & medicinal chemistry letters》2012,22(23):7135-7141
Novel small molecule antagonists of NPBWR1 (GPR7) are herein reported. A high-throughput screening (HTS) of the Molecular Libraries-Small Molecule Repository library identified 5-chloro-4-(4-methoxyphenoxy)-2-(p-tolyl)pyridazin-3(2H)-one as a NPBWR1 hit antagonist with micromolar activity. Design, synthesis and structure–activity relationships study of the HTS-derived hit led to the identification of 5-chloro-2-(3,5-dimethylphenyl)-4-(4-methoxyphenoxy)pyridazin-3(2H)-one lead molecule with submicromolar antagonist activity at the target receptor and high selectivity against a panel of therapeutically relevant off-target proteins. This lead molecule may provide a pharmacological tool to clarify the molecular basis of the in vivo physiological function and therapeutic utility of NPBWR1 in diverse disease areas including inflammatory pain and eating disorders. 相似文献
90.
Crescioli C Sottili M Bonini P Cosmi L Chiarugi P Romagnani P Vannelli GB Colletti M Isidori AM Serio M Lenzi A Di Luigi L 《European journal of cell biology》2012,91(2):139-149
Inflammatory myopathies (IMs) are systemic diseases characterized by a T helper (Th) 1 type inflammatory response and cell infiltrates within skeletal muscles. The mainstay of treatment is drugs aimed at suppressing the immune system - corticosteroids and immunosuppressants. About 25% of patients are non-responders. Skeletal muscle cells seem actively involved in the immune-inflammatory response and not only a target; understanding the molecular bases of IMs might help drug development strategies. Within muscles the interaction between the chemokine interferon (IFN)γ inducible 10 kDa protein, CXCL10 or IP-10, and its specific receptor CXCR3, present on Th1 type infiltrating cells, likely plays a pivotal role, potentially offering the opportunity for therapeutic intervention. We aimed to clarify the involvement of human skeletal muscle cells in inflammatory processes in terms of CXCL10 secretion, to elucidate the engaged molecular mechanism(s) and, finally, to evaluate muscular cell responses, if any, to some immunosuppressants routinely used in IM treatment, such as methylprednisolone, methotrexate, cyclosporin A and Infliximab. We first isolated and characterized human fetal skeletal muscle cells (Hfsmc), which expressed the specific lineage markers and showed the competence to react in the context of an in vitro alloresponse. CXCL10 protein secretion by Hfsmc was similarly induced by the inflammatory cytokines interferon (IFN)γ and tumor necrosis factor (TNF)α, above undetectable control levels, through the activation of Stat1 and NF-kB pathways, respectively; CXCL10 secretion was significantly magnified by cytokine combination, and this synergy was associated to a significant up-regulation of TNFαRII; cytokine-induced CXCL10 secretion was considerably affected only by Infliximab. Our data suggested that human skeletal muscle cells might actively self-promote muscular inflammation by eliciting CXCL10 secretion, which is known to amplify Th1 cell tissue infiltration in vivo. In conclusion, we sustain that pharmacological targeting of CXCL10 within muscular cells might contribute to keep in control pro-Th1 polarization of the immune/inflammatory response. 相似文献